chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121541169315411694AC20GENIChomozygous50073010
121541199515411996AG18GENIChomozygous50073012
121541210115412102GGA22GENICpossibly homozygous50073014
121541702215417023TC24GENIChomozygous50073016
121541703715417041AGTG----23GENIChomozygous50073018
121541769015417691CG13GENIChomozygous50073020
121541769615417697TC12GENIChomozygous50073022
121541770915417710TA12GENIChomozygous50073024
121541772415417725GGA11GENIChomozygous50073026
121541773715417738A-2GENIChomozygous50560589
121541898215418983TTA18GENIChomozygous50073034
121541916215419163AC22GENIChomozygous50073036
121542008115420082GA28GENIChomozygous50073038
121542008315420084GA29GENIChomozygous50282106
121542008515420086AG29GENIChomozygous50282107
121542034715420348CT23GENIChomozygous50073040
121542081215420813GA21GENIChomozygous50073042
121542082715420828GA24GENIChomozygous50073044
121542103215421033TA13GENIChomozygous50073046
121542103515421036TG14GENIChomozygous50073048
121542104015421041AC16GENIChomozygous50073050
121542104415421045AG15GENIChomozygous50073052
121542104915421050TA17GENIChomozygous50504038
121542105015421051CA17GENIChomozygous50504039
121542105215421053GC17GENIChomozygous50504040
121542105615421057AC18GENIChomozygous50073054
121542106415421065TA21GENIChomozygous50073056
121542114515421146GGCTCGTCTGGACGCTCTCTATCTTGTCT27GENIChomozygous50504041
121542170615421707CT24GENIChomozygous50073058
121542194615421947AC32GENIChomozygous50073060
121542211215422113TC16GENIChomozygous50073062
121542241515422416GA19GENIChomozygous50073064
121542246915422470A-14GENIChomozygous50073066
121542296015422961TC21GENIChomozygous50073068
121542298515422986AG20GENIChomozygous50073070
121542373815423743AACAA-----7GENIChomozygous50533712
121542408515424086CT12GENIChomozygous50073074
121542418015424181GA14GENIChomozygous50073076
121542468015424681TG2GENIChomozygous50073078
121542469415424695CT3GENIChomozygous50073080